Utilizing open-source platforms to build and deploy interactive patient-reported quality of life tracking tools for monitoring protocol adherence
Author:
Publisher
Springer Science and Business Media LLC
Subject
Public Health, Environmental and Occupational Health
Link
https://link.springer.com/content/pdf/10.1007/s11136-020-02617-z.pdf
Reference16 articles.
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2. Smith, A. W., Mitchell, S. A., De Aguiar, C. K., Moy, C., Riley, W. T., Wagster, M. V., et al. (2016). News from the NIH: Person-centered outcomes measurement: NIH-supported measurement systems to evaluate self-assessed health, functional performance, and symptomatic toxicity. Translational Behavioral Medicine, 6(3), 470–474. https://doi.org/10.1007/s13142-015-0345-9.
3. Bottomley, A., Pe, M., Sloan, J., Basch, E., Bonnetain, F., Calvert, M., et al. (2016). Analysing data from patient-reported outcome and quality of life endpoints for cancer clinical trials: A start in setting international standards. The Lancet Oncology, 17(11), e510–e514. https://doi.org/10.1016/S1470-2045(16)30510-1.
4. Mercieca-Bebber, R., Palmer, M. J., Brundage, M., Calvert, M., Stockler, M. R., & King, M. T. (2016). Design, implementation and reporting strategies to reduce the instance and impact of missing patient-reported outcome (PRO) data: A systematic review. British Medical Journal Open, 6(6), e010938. https://doi.org/10.1136/bmjopen-2015-010938.
5. May, M. (2019). Twenty-five ways clinical trials have changed in the last 25 years. Exploring the evolution, from analysis and endpoints to registration and regulations. Nature Medicine, 25(1), 2–5. https://doi.org/10.1038/s41591-018-0314-1.
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